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Large-scale copy number variants (CNVs) detected in different ethnic human populations

机译:在不同种族人群中发现的大规模拷贝数变异(CNV)

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摘要

The large-scale copy-number variations (CNVs) in the human genome are associated with develop-mental disorders and susceptibility to diseases. More im-portantly, CNVs may represent a major genetic component of our phenotypic diversity. Following the development of methodologies and introduction of new research platforms, accumulation of the nature and pattern of CNVs from normal populations has progressed. The examination of relatively large numbers of specific ethnic groups has recently started. Although the results are not always consistent, it is likely that different human populations bear different CNVs, as is the case for single-nucleotide polymorphisms (SNPs) and insertion-deletion (indel) polymorphisms. We review recent publications about the nature of inter-population, especially inter-ethnic group, differences of CNVs.
机译:人类基因组中的大规模拷贝数变异(CNV)与心理发展障碍和疾病易感性有关。更重要的是,CNV可能代表了我们表型多样性的主要遗传成分。随着方法学的发展和新研究平台的引入,来自正常人群的CNV的性质和模式的积累已取得进展。最近已经开始对相对大量的特定种族进行检查。尽管结果并不总是一致的,但不同的人群可能携带不同的CNV,如单核苷酸多态性(SNP)和插入缺失(indel)多态性。我们回顾了有关人群之间,尤其是种族间群体,CNV差异的性质的最新出版物。

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