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Article

A Genome-Wide Association Study to Identify Potential Germline Copy Number Variants for Sporadic Breast Cancer Susceptibility.

Cytogenetic and genome research - 1 Jan 2016

Sapkota Yadav, Narasimhan Ashok, Kumaran Mahalakshmi, Sehrawat Badan S, Damaraju Sambasivarao

Abstract excerpt

Breast cancer (BC) predisposition in populations arises from both genetic and nongenetic risk factors. Structural variations such as copy number variations (CNVs) are heritable determinants for disease susceptibility. The primary objectives of this study are (1) to identify CNVs associated with sporadic BC using a genome-wide association study (GWAS) design; (2) to utilize 2 distinct CNV calling algorithms to...

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Identifiers

PMID: 27668787
DOI: 10.1159/000448558

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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