To understand the role of CNVs across human diseases, we examine the CNV genomic landscape of 100,028 unrelated individuals of European ancestry, using SNP and CGH array datasets. Nature Communications volume 11, Article number: 255 ( 2020)Ĭopy number variants (CNVs) are suggested to have a widespread impact on the human genome and phenotypes. Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
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