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Table 2 NEGR1 and BTNL8-BTNL3 deletions in population controls

From: Ancestry and frequency of genetic variants in the general population are confounders in the characterization of germline variants linked to cancer

 

NEGR1 deletion

BTNL8-BTNL3 deletion

Homozygous

Heterozygous

Homozygous

Heterozygous

European (n = 2101)

36.4%

50.1%

8.6%

42.7%

East Asian (n = 118)

80.5%

16.9%

1.7%

37.3%

South East Asian (n = 80)

42.5%

50.0%

2.5%

15.0%

African (n = 42)

14.3%

57.1%

2.4%

21.4%

American (n = 53)

49.1%

47.2%

11.3%

39.6%

Other (n = 202)

44.6%

41.6%

4.0%

30.7%

  1. Frequencies of the control collection (n = 2596) stratified by ethnic groups and homozygous or heterozygous deletion types