Single mutations & LOH regions

Fragile sites

1p13.3

3p24

5q35.1

5q35.3

6q23-27

8p22.1-24

8p22.1-q24.12

9p12-p34

10q24-26

11p15.5

11q31-q24.2

13q13

15q14-q23

16p-,

17p13.1

17p11.2

Centric white band—Gene symbol KCND3-FRA1p13.3

FRA3A-p24

FRA5-q31

FRA5q-25.3

FRA6E-q26-8p2.1

FRA8B-p22-9q21

LOH region uniparental disomy—FRA sites 8B-p22 & 8B-p12

FRA9D-p22.1 & Eq32-31—Inclusive of CDKN2A

FRA10E-q25.2 & FRA10F-q24-26.3

FRA11C-p15.1

FRA11F-q14.2-q24.2 & FRA11F-q14.2

FRA13A-q13

FRA15A-q22.1

Loss of p-arm (centromere breakage)

White band near tip of p-arm

Location of TP53 17p11.2

& two losses of the 9p arm affecting functional loss of p16ink4a gene and others