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Article

Concurrent copy number variations on chromosome 8 and 22 combined with mutation at FGA locus revealed in a parentage testing case.

Forensic science international. Genetics - 1 Nov 2015

Yang Yaran, Ren He, Chen Wei, Xie Bingbing, Wang Yan, Shi Yan, Chen Chong, Li Chen, Yi Le, Fang Xiangdong, Yan Jiangwei

Abstract excerpt

Copy number variations (CNVs) are one of the major sources of human genetic diversity and are associated with rare genomic disorders as well as complex traits and diseases. A copy number variation was observed at the D8S1179 locus during routine STR based parentage testing, in which the child exhibited three alleles, "13, 15, 16", with the putative father a homozygous "15" and the mother homozygous "13". In...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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PMID: 26186693
DOI: 10.1016/j.fsigen.2015.07.002

Genes

FGA

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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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