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Table 2 Burden analysis of CNV Regions reveals a higher number of CNVs in genes in individuals with narrow bipolar phenotype (BPI and BPII)

From: Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

 

Unaffected

Broad

Narrow

No. All CNVs

28.1

28.7

29.5

P vs unaffected

-

0.39

0.26

No. All CNVs in genes

15.6

16.8

17.3

P vs unaffected

-

0.16

0.11

No. Rare CNVs in genes

9.7

11.0

11.3

P vs unaffected

-

0.12

0.09

No. CNVs in disease genes

4.8

5.5

5.7

P vs unaffected

-

0.11

0.06

No. Rare CNVs in disease genes

4.0

4.8

5.0

P vs unaffected

-

0.07

0.06

  1. A trend towards an increased number of CNVs in disease genes in individuals with narrow bipolar phenotype is also reported.
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BMC Genomic Data

ISSN: 2730-6844

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