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Table 3 The CNVs and the rank of occurrences found in targeted deafness genes among the 79 patient samples

From: Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness

Gene name

Chromosome number

# of occurrence of CNVs

DIAPH1

Chr5

16

COL11A2

Chr6

15

MYO1C

Chr17

12

STRC

Chr15

8

OTOA

Chr16

6

MYO3A

Chr10

5

ERCC2

Chr19

4

USH1C

Chr11

4

GRHL2

Chr8

3

MYO6

Chr6

3

CDH23

Chr10

2

MYH14

Chr19

2

MYO15A

Chr17

2

MYO7A

Chr11

2

SOX2

Chr3

2

COCH

Chr14

1

COL9A3

Chr20

1

CATSPER2

Chr15

1

DFNA5

Chr7

1

DFNB59

Chr2

1

EYA4

Chr6

1

LHX3

Chr9

1

MTAP

Chr9

1

OTOR

Chr20

1

SLC26A4

Chr7

1

SLC26A11

Chr17

1

TMPRSS5

Chr11

1

GJB3

Chr1

1