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Article

Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies.

Journal of human genetics - 1 Jan 2021

Nakatochi Masahiro, Kushima Itaru, Ozaki Norio

Abstract excerpt

Copy number variants (CNVs), defined as genome sequences of ≥50 bp that differ in copy number from that in a reference genome, are a common form of structural variation. Germline CNVs account for some of the missing heritability that single nucleotide polymorphisms could not account for. Recent technological advances have had a huge impact on CNV research. Microarray technology enables relatively low-cost,...

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PMID: 32958875
DOI: 10.1038/s10038-020-00838-1

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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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