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Article

Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia.

PloS one - 1 Jan 2014

Mokhtar Siti Shuhada, Marshall Christian R, Phipps Maude E, Thiruvahindrapuram Bhooma, Lionel Anath C, Scherer Stephen W, Peng Hoh Boon

Abstract excerpt

Copy number variation (CNV) has been recognized as a major contributor to human genome diversity. It plays an important role in determining phenotypes and has been associated with a number of common and complex diseases. However CNV data from diverse populations is still limited. Here we report the first investigation of CNV in the indigenous populations from Peninsular Malaysia. We genotyped 34 Negrito genomes...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 24956385
DOI: 10.1371/journal.pone.0100371
PMCID: PMC4067311

Provenance

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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