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Table 3 Genes associated with unique CNVs identified across multiple patients

From: Expanding the genetic basis of copy number variation in familial breast cancer

 

Number of Patients

Gene

Loci

Gains

2

B2M

15q21.1

 

2

DSCAM

21q22.2

 

2

G0S2

1q32.2

 

2

GNG2

14q22.1

 

2

GPR98

5q14.3

 

2

IL8

4q13.3

 

2

LAMB3

1q32.2

 

2

LIMS1

2q13

 

2

NBN

8q21.3

 

2

TAGAP

6q25.3

 

2

TRIM69

15q21.1

Both

2

CNTN4

3p26.3

 

2

IMMP2L

7q31.1

 

2

WWOX

16q23.1

Losses

2

ACYP2

2p16.2

 

2

PCDH9

13q21.32

 

2

SPINT4

20q13.12

 

2

TSPYL6

2p16.2

 

2

VAV3

1p13.3

 

3

PIK3R5

17p13.1

 

3

POU2F3

11q23.3

 

4

ARHGEF12

11q23.3

 

4

TMEM136

11q23.3

 

5

NAMPT

7q22.2

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Hereditary Cancer in Clinical Practice

ISSN: 1897-4287