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High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications
(Cold Spring Harbor Laboratory Press, 2009-09-19)
We present a database of copy number variations (CNVs) detected in 2026 disease-free individuals, using high-density, SNP-based oligonucleotide microarrays. This large cohort, comprised mainly of Caucasians (65.2%) and ...