Copy number variation in human genomes from three major ethno-linguistic groups in Africa.

BMC Genomics · 2020 · PMC7147055 · PMID 32272904

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highly significantno p-value reported

However, it should be noted that although there was a highly significant excess of CNVRs with SNPs that tagged CNVs and SNPs that had evidence of selection, the 32% excess of SNPs that were both Tag SNP and had evidence of selection was not significant.

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