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Widening the spectrum of human genetic variation

被引：72
作者：
Eichler, EE [1 ]
机构：
[1] Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
来源：
NATURE GENETICS | 2006年 / 38卷 / 01期
关键词：
D O I：
10.1038/ng0106-9
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
SNP genotyping platforms have been used to discover similar to 1,000 deletion structural variants within the human genome, with median lengths ranging from 500 bp to 10.5 kb. Analyses of a subset of these provide compelling evidence of linkage disequilibrium with flanking SNPs.
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页码：9 / 11
页数：3
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