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Article

High-resolution SNP microarray investigation of copy number variations on chromosome 18 in a control cohort.

Cytogenetic and genome research - 1 Jan 2013

Chia N L, Bryce M, Hickman P E, Potter J M, Glasgow N, Koerbin G, Danoy P, Brown M A, Cavanaugh J

Abstract excerpt

Copy number variations (CNVs) as described in the healthy population are purported to contribute significantly to genetic heterogeneity. Recent studies have described CNVs using lymphoblastoid cell lines or by application of specifically developed algorithms to interrogate previously described da...

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Share to Chromosome Duplication
Share to Chromosomes, Human, Pair 18
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23635498
DOI: 10.1159/000350767

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23635498-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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