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 |