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A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.

Animal genetics - 1 Jun 2015

Wu Yang, Fan Huizhong, Jing Shengyun, Xia Jiangwei, Chen Yan, Zhang Lupei, Gao Xue, Li Junya, Gao Huijiang, Ren Hongyan

Abstract excerpt

Copy number variations (CNVs) have recently been identified as promising sources of genetic variation, complementary to single nucleotide polymorphisms (SNPs). As a result, detection of CNVs has attracted a great deal of attention. In this study, we performed genome-wide CNV detection using Illumina Bovine HD BeadChip (770k) data on 792 Simmental cattle. A total of 263 CNV regions (CNVRs) were identified, which...

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PMID: 25917301
DOI: 10.1111/age.12288

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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