Penetrance, effect and causal attribution: which number should be reported for recurrent copy-number variants?

Penetrance has a conventional and clinically useful meaning: among carriers of a genetic variant, what proportion manifest a specified phenotype? Goh et al. have identified a genuine problem in recurrent copy-number variant (CNV) counselling: historical estimates may be distorted by the assumed background prevalence of intellectual disability, ascertainment and clinically enriched cohorts. Their revised analysis of 83 recurrent CNVs is therefore an important corrective [ 1 , 2 , 3 ].

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Publication Details

Journal
European Journal of Human Genetics
Published
2026-09-18
DOI
https://doi.org/10.1038/s41431-026-02236-1
Primary Topic
Genomic variations and chromosomal abnormalities
Type
article
Field-Weighted Citation Impact
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article

Penetrance, effect and causal attribution: which number should be reported for recurrent copy-number variants?

Himanshu Goel
European Journal of Human Genetics
Genomic variations and chromosomal abnormalities
article

Penetrance, effect and causal attribution: which number should be reported for recurrent copy-number variants?

Himanshu Goel
article en

Abstract

Penetrance has a conventional and clinically useful meaning: among carriers of a genetic variant, what proportion manifest a specified phenotype? Goh et al. have identified a genuine problem in recurrent copy-number variant (CNV) counselling: historical estimates may be distorted by the assumed background prevalence of intellectual disability, ascertainment and clinically enriched cohorts. Their revised analysis of 83 recurrent CNVs is therefore an important corrective [ 1 , 2 , 3 ].

European Journal of Human Genetics
Hunter Genetics (AU), University of Newcastle Australia (AU)
Openalex Percentile: Top 11%
Genomic variations and chromosomal abnormalities
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