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Article

Prediction of a deletion copy number variant by a dense SNP panel.

Genetics, selection, evolution : GSE - 23 Mar 2012

Kadri Naveen K, Koks Patrick D, Meuwissen Theo H E

Abstract excerpt

BACKGROUND: A newly recognized type of genetic variation, Copy Number Variation (CNV), is detected in mammalian genomes, e.g. the cattle genome. This form of variation can potentially cause phenotypic variation. Our objective was to determine whether dense SNP (single nucleotide polymorphisms) panels can capture the genetic variation due to a simple bi-allelic CNV, with the prospect of including the effect of...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22443295
DOI: 10.1186/1297-9686-44-7
PMCID: PMC3366870

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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