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Da Silva et al. BMC Genomics (2018) 19:195 https://doi.org/10.1186/s1286401845771RESEARCH ARTICLEOpen Accessing are associated with genomic architecture in a songbird Vinicius H. the Silva1,2,3×,
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CNVs are associated with Copy Number Variations, which are changes in the number of copies of a particular gene or DNA segment in the genome.
Researchers, geneticists, and healthcare professionals are required to file CNVs associated with their studies or patient cases.
CNVs are filled out by documenting the specific gene or DNA segment, indicating the detected copy number variations, and providing relevant clinical or research data.
The purpose of CNVs associated with is to understand genetic variations and their potential impact on health or disease.
Information reported on CNVs associated with includes the gene or DNA segment affected, the type and extent of copy number variations, and any relevant clinical or research findings.
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