22;68
2Lt - 22D1 | 33F5 - 32 | 68 - 61C | 74 - 89D | 93B - 96B | 61A - 3Lt; 3Rt - 96A | 93B - 89E | 74 - 68 | 32 - 22D2 | 34A1 - 42A2 | 58A4 - 42A3 | 58B1 - 2Rt
32;68;[32-32];[68-68];
Homozygous lethal because of the dominant markers in the component balancers.
This is a spontaneous translocation that arose in a In(2L)Cy In(2R)Cy; TM2 stock (FBrf0017412, FBrf0066905). It carries a T(2;3) translocation (32;68) between a second chromosome carrying In(2L)Cy (22D1-2;33F5-34A1) and In(2R)Cy (42A2-3;58A4) and TM2 (61A-C;74;89E1-2;93B;96A).
Induced on: In(2L)Cy In(2R)Cy In(3LR)Ubx130.
Segregates as a unit and suppresses recombination in chromosomes 2 and 3.
All limits from polytene analysis (citation unavailable)