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Article

Identification of rare germline copy number variations over-represented in five human cancer types.

Molecular cancer - 3 Feb 2015

Park Richard W, Kim Tae-Min, Kasif Simon, Park Peter J

Abstract excerpt

BACKGROUND: Copy number variations (CNVs) are increasingly recognized as significant disease susceptibility markers in many complex disorders including cancer. The availability of a large number of chromosomal copy number profiles in both malignant and normal tissues in cancer patients presents an opportunity to characterize not only somatic alterations but also germline CNVs, which may confer increased risk for...

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PMID: 25644941
DOI: 10.1186/s12943-015-0292-6
PMCID: PMC4381456

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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