Table 2 Prevalence estimates of recurrent NDD CNVs spanning 13 regions associated with neurodevelopmental disorders.

From: Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents

Recurrent CNVs

De novo CNVs

Maternal CNVs

Paternal CNVs

All CNVs

Position (hg37)

Description

Length (Mb)

N

Prev (95% C.I.)

Inheritance status

N

Prev (95% C.I.)

N

Prev (95% C.I.)

N

Prev (95% C.I.)

1:146578858:147396590

1q21.1:Del

0.817732

2

1.63 (0.45, 5.95)

Paternal x2

3

2.45 (0.83, 7.2)

1

0.82 (0.14, 4.62)

6

4.9 (2.24, 10.68)

1:146578858:147396590

1q21.1:Dup

0.817732

0

0

 

4

3.26 (1.27, 8.39)

0

0

4

3.26 (1.27, 8.39)

3:195759926:197346552

3q29:Del

1.586626

1

0.82 (0.14, 4.62)

Paternal

0

0

0

0

1

0.82 (0.14, 4.62)

3:195759926:197346552

3q29:Dup

1.586626

0

0

 

0

0

0

0

0

0

7:72745828:74145433

7q11.23 (Williams-Beuren):Del

1.399605

0

0

 

0

0

0

0

0

0

7:72745828:74145433

7q11.23:Dup

1.399605

0

0

 

0

0

0

0

0

0

15:22754735:28570518

15q11.2–13.1 (Prader–Willi/Angelman):Del

5.815783

0

0

 

0

0

0

0

0

0

15:22754735:28570518

15q11.2–13.1:Dup*

5.815783

2

1.63 (0.45, 5.95)

Maternal x2*

1

0.82 (0.14, 4.62)

0

0

3

2.45 (0.83, 7.2)

15:31075791:32446853

15q13.3:Del

1.371062

1

0.82 (0.14, 4.62)

Paternal

3

2.45 (0.83, 7.2)

1

0.82 (0.14, 4.62)

5

4.08 (1.74, 9.55)

15:31075791:32446853

15q13.3:Dup

1.371062

1

0.82 (0.14, 4.62)

Paternal

2

1.63 (0.45, 5.95)

3

2.45 (0.83, 7.2)

6

4.9 (2.24, 10.68)

16:28823089:29046734

16p11.2 distal:Del

0.223645

1

0.82 (0.14, 4.62)

Maternal

1

0.82 (0.14, 4.62)

1

0.82 (0.14, 4.62)

3

2.45 (0.83, 7.2)

16:28823089:29046734

16p11.2 distal:Dup§

0.223645

2

1.63 (0.45, 5.95)

Maternal unknown§

1

0.82 (0.14, 4.62)

5

4.08 (1.74, 9.55)

8

6.53 (3.31, 12.88)

16:29650744:30195048

16p11.2 proximal:Del

0.544304

4

3.26 (1.27, 8.39)

Maternal x3 paternal

2

1.63 (0.45, 5.95)

0

0

6

4.9 (2.24, 10.68)

16:29650744:30195048

16p11.2 proximal:Dup

0.544304

0

0

 

4

3.26 (1.27, 8.39)

1

0.82 (0.14, 4.62)

5

4.08 (1.74, 9.55)

17:1247834:2588909

17p13.3 (YWHAE, PAFAH1B, Miller-Dieker syndrome):Del

1.341075

0

0

 

0

0

0

0

0

0

17:1247834:2588909

17p13.3 (YWHAE, PAFAH1B1):Dup

1.341075

0

0

 

0

0

0

0

0

0

17:16811743:20216832

17p11.2 (Smith-Magenis):Del

3.405089

0

0

 

0

0

0

0

0

0

17:16811743:20216832

17p11.2 (Potocki-Lupski):Dup

3.405089

0

0

 

0

0

0

0

0

0

17:34816572:36215672

17q12:Del

1.3991

3

2.45 (0.83, 7.2)

Maternal paternal x2

0

0

0

0

3

2.45 (0.83, 7.2)

17:34816572:36215672

17q12:Dup

1.3991

0

0

 

1

0.82 (0.14, 4.62)

1

0.82 (0.14, 4.62)

2

1.63 (0.45, 5.95)

17:43706119:44165156

17q21.31 (Koolen-de Vries):Del

0.459037

0

0

 

0

0

0

0

0

0

17:43706119:44165156

17q21.31:Dup

0.459037

0

0

 

0

0

0

0

0

0

22:19024860:21469135

22q11.2 (DiGeorge):Del

2.444275

1

0.82 (0.14, 4.62)

Maternal

0

0

0

0

1

0.82 (0.14, 4.62)

22:19024860:21469135

22q11.2:Dup

2.444275

2

1.63 (0.45, 5.95)

Maternal paternal

2

1.63 (0.45, 5.95)

2

1.63 (0.45, 5.95)

6

4.9 (2.24, 10.68)

22:21920486:23652202

22q11.2 distal:Del

1.731716

0

0

 

0

0

0

0

0

0

22:21920486:23652202

22q11.2 distal:Dup

1.731716

0

0

 

0

0

0

0

0

0

 

Total

 

20

16.32 (10.57, 25.2)

 

24

19.59 (13.17, 29.13)

15

12.24 (7.42, 20.19)

59

48.16 (37.35, 62.06)

  1. N counts, Prev prevalence in 10,000.
  2. *Indicates that one of the de novo duplications is mosaic and of maternal origin, §indicates that we could not assess the origin of one de novo variant.