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Genome-wide Analysis of Common Copy Number Variation and Epithelial Ovarian Cancer Risk

4 Apr 2019

Abstract excerpt

Abstract Background: Germline DNA copy number variation (CNV) is a ubiquitous source of genetic variation and remains largely unexplored in association with epithelial ovarian cancer (EOC) risk. Methods: CNV was quantified in the DNA of approximately 3,500 cases and controls genotyped with the Illumina 610k and HumanOmni2.5M arrays. We performed a genome-wide association study of common (>1%) CNV regions (CNVRs)...

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PMID: 30948450
DOI: 10.1158/1055-9965.epi-18-0833

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