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Table 1 Frequency of CG-CNVs in general human population

From: Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants

Kind of aberration

Frequency [%]

inv(9)(p11q13)

2.86

acrocentric p+

2.38

Yqh+

0.78

16qh+

0.37

9qh+

0.33

1qh+

0.25

acrocentric p-

0.11

inv(2)(p11.2q13)

0.11

Yqh-

0.09

  1. The data was adapted from [15]
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Molecular Cytogenetics

ISSN: 1755-8166