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copy number variation
noun
The variation of the number of copies (normally two) of a gene, or of sequences of DNA, in the genome of a specific individual; has been linked to some diseases
Exact(60)
Copy number variation plays an important role in clinical epilepsy.
Hannibal, R. L. et al. Copy number variation is a fundamental aspect of the placental genome.
Krumm, N. et al. Copy number variation detection and genotyping from exome sequence data.
Cheeseman, I. H. et al. Gene copy number variation throughout the Plasmodium falciparum genome.
Sudmant, P.H. et al. Diversity of human copy number variation and multicopy genes.
SCNAs were detected using Recapseg34, and allele-specific copy number variation was detected using AllelicCapseg.
Sudmant, P. H. et al. Diversity of human copy number variation and multicopy genes.
Cho, E.K. et al. Array-based comparative genomic hybridization and copy number variation in cancer research.
Conrad, D.F. et al. Origins and functional impact of copy number variation in the human genome.
Diskin, S.J. et al. Copy number variation at 1q21.1 associated with neuroblastoma.
Mills, R.E. et al. Mapping copy number variation by population-scale genome sequencing.
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