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.

引用

页码：9 / 11

页数：3

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