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Article

Copy number variation accuracy in genome-wide association studies.

Human heredity - 1 Jan 2011

Lin Peng, Hartz Sarah M, Wang Jen-Chyong, Krueger Robert F, Foroud Tatiana M, Edenberg Howard J, Nurnberger John I, Brooks Andrew I, Tischfield Jay A, Almasy Laura, Webb Bradley T, Hesselbrock Victor M, Porjesz Bernice, Goate Alison M, Bierut Laura J, Rice John P

Abstract excerpt

BACKGROUND/AIM: Copy number variations (CNVs) are a major source of alterations among individuals and are a potential risk factor in many diseases. Numerous diseases have been linked to deletions and duplications of these chromosomal segments. Data from genome-wide association studies and other m...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 21778733
DOI: 10.1159/000324683
PMCID: PMC3153341

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21778733-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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