Eichler, E.E. Widening the spectrum of human genetic variation. Nat. Genet. 38, 9-11

ArticleinNature Genetics 38(1):9-11 · February 2006with6 Reads
Impact Factor: 29.35 · DOI: 10.1038/ng0106-9 · Source: PubMed

    Abstract

    SNP genotyping platforms have been used to discover -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.