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Table 1 Significantly associated regions detected by CNstream and PennCNV

From: CNstream: A method for the identification and genotyping of copy number polymorphisms using Illumina microarrays

REGIONS

CHROM

BASEPAIR

DELS CASES

DELS CONTROLS

OR

   

N

%

n

%

 

CNSTREAM SIGNIFICANT SEGMENTS

8p22

8

15435527..15453141

24

7.2

4

2.6

2.9

 

8

15439515..15455979

33

9.9

5

3.3

3.2

 

8

15447669..15464497

33

9.9

5

3.3

3.2

 

8

15450330..15467035

24

7.2

4

2.6

2.9

19p12

19

20368239..20449621

51

15.2

11

7.2

2.3

 

19

20385941..20473895

54

16.1

11

7.2

2.5

 

19

20423788..20520617

54

16.1

11

7.2

2.5

 

19

20439390..20522325

40

11.9

5

3.3

4

PENNCNV SIGNIFICANT PROBES

8q24.3

8

145079175

30

9.0

0

0.0

Inf

 

8

145083192

30

9.0

0

0.0

Inf

 

8

145083193

29

8.7

0

0.0

Inf

 

8

145090342

29

8.7

0

0.0

Inf

11p15.5

11

1073364

16

4.8

2

1.3

3.8

 

11

1074362

16

4.8

2

1.3

3.8

 

11

1074363

15

4.5

2

1.3

3.5

 

11

1086494

15

4.5

2

1.3

3.5

19p13.3

19

4020119

15

4.5

1

0.7

7.1

 

19

4028096

15

4.5

1

0.7

7.1

 

19

4037807

15

4.5

1

0.7

7.1

 

19

4041113

15

4.5

1

0.7

7.1

  1. Number and percentage of cases and controls in each of the associated CNP regions detected by CNstream and PennCNV. In bold, the candidate regions chosen for quantitative PCR validation.