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Table 2 Average CNV frequency within 1 Mbp of different genomic regions

From: Understanding genetic variability: exploring large-scale copy number variants through non-invasive prenatal testing in European populations

Region

Slovak

Czech

Hungarian

Average

1 Mbp of random haploid genome sequence

0.040%

0.038%

0.044%

0.041%

1 Mbp proximal to centromere

5.76%

7.04%

12.66%

8.48%

1 Mbp proximal to telomeres

7.31%

7.41%

8.39%

7.70%