Description:
                                                    
                                                    
                                                         
                                                            
                                                            HUMAN VARIATION PANEL - NORTHERN EUROPEAN 
                                                            
                                                    
                                                 
                                                
                                                
                                                
                                                
                                             
                                         
                                     
                                    
                                        
                                            
                                            
                                            
                                            
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
                                                                    
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                                                                            Repository
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                                                                            NIGMS Human Genetic Cell Repository
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	| Subcollection | 
	Human Variation | 
 
                                                                
                                                                
                                                                
                                                                
	| Alternate IDs | 
	GM11814 [HUMAN VARIATION PANEL - NORTHERN EUROPEAN] | 
 
                                                                
                                                                
	| Quantity | 
	25 µg | 
 
	| Quantitation Method | 
	Please see our FAQ | 
 
                                                                
                                                                    
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                                                                            Biopsy Source
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                                                                            Peripheral vein
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                                                                            Cell Type
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                                                                            B-Lymphocyte
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                                                                            Tissue Type
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                                                                            Blood
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                                                                            Transformant
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                                                                            Epstein-Barr Virus
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                                                                            Sample Source
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                                                                            DNA from LCL
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                                                                        | 
                                                                            Species
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                                                                            Homo sapiens
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                                                                        | 
                                                                            Common Name
                                                                         | 
                                                                        
                                                                            Human
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	| IDENTIFICATION OF SPECIES OF ORIGIN | 
	Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis | 
 
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	| Mun S, Kim S, Lee W, Kang K, Meyer TJ, Han BG, Han K, Kim HS, A study of transposable element-associated structural variations (TASVs) using a de novo-assembled Korean genome Experimental & molecular medicine53:615-630 2019 | 
 
	| PubMed ID: 33833373 | 
 
	|   | 
 
	| Wernstedt A, Valtorta E, Armelao F, Togni R, Girlando S, Baudis M, Heinimann K, Messiaen L, Staehli N, Zschocke J, Marra G, Wimmer K, Improved multiplex ligation-dependent probe amplification analysis identifies a deleterious PMS2 allele generated by recombination with crossover between PMS2 and PMS2CL Genes, chromosomes & cancer51:819-31 2012 | 
 
	| PubMed ID: 22585707 | 
 
	|   | 
 
	| Wang X, Abudu A, Son S, Dang Y, Venta PJ, Zheng YH, Analysis of Human APOBEC3H Haplotypes and Anti-Human Immunodeficiency Virus Type-1 Activity Journal of virology85(7):3142-52 2011 | 
 
	| PubMed ID: 21270145 | 
 
	|   | 
 
	| Londin ER, Keller MA, Maista C, Smith G, Mamounas LA, Zhang R, Madore SJ, Gwinn K, Corriveau RA.
, CoAIMs: A Cost-Effective Panel of Ancestry Informative Markers for Determining Continental Origins.
 Plos One5(10):e13443 2010 | 
 
	| PubMed ID: 20976178 | 
 
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	| Marini NJ, Gin J, Ziegle J, Keho KH, Ginzinger D, Gilbert DA, Rine J, The prevalence of folate-remedial MTHFR enzyme variants in humans Proceedings of the National Academy of Sciences of the United States of America5(10):e13443 2008 | 
 
	| PubMed ID: 18523009 | 
 
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	| Awomoyi A, Sirugo G, Newport MJ, Tishkoff S, Global distribution of a novel trinucleotide microsatellite polymorphism (ATA)n in intron 8 of the SLC11A1 gene and susceptibility to pulmonary tuberculosis International journal of immunogenetics33:11-5 2006 | 
 
	| PubMed ID: 16426236 | 
 
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	| Hurley JD, Engle LJ, Davis JT, Welsh AM, Landers JE, A simple, bead-based approach for multi-SNP molecular haplotyping Nucleic acids research32:e186 2005 | 
 
	| PubMed ID: 15637233 | 
 
	|   | 
 
	| Wang J, Song L, Gonder MK, Azrak S, Ray DA, Batzer MA, Tishkoff SA, Liang P, Whole genome computational comparative genomics: A fruitful approach for ascertaining Alu insertion polymorphisms Gene365:11-20 2005 | 
 
	| PubMed ID: 16376498 | 
 
                                                                
                                                             
                                                            
                                                         
                                                     
                                                 
                                                
                                                
                                                
                                             
                                         
                                     
                                 
                                
                             
                         
                     
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