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Article

Advantage of using allele-specific copy numbers when testing for association in regions with common copy number variants.

PloS one - 1 Jan 2013

Marenne Gaëlle, Chanock Stephen J, Malats Núria, Génin Emmanuelle

Abstract excerpt

Copy number variants (CNV) can be called from SNP-arrays; however, few studies have attempted to combine both CNV and SNP calls to test for association with complex diseases. Even when SNPs are located within CNVs, two separate association analyses are necessary, to compare the distribution of bi...

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PMID: 24040408
DOI: 10.1371/journal.pone.0075350
PMCID: PMC3769257

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24040408-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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