[95A1-95A1];[95A4-95A4];
A set of ~800 largely isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Designed to fill gaps in deletion coverage and breakpoint placement; also used to replace older available deficiencies that have not been molecularly mapped.
95A1;95A4
Breakpoint based on release 3 sequence coordinate from Thibault et al., 2004, Supplementary Table 2 (FBrf0174227) or 3 (FBrf0174228), converted to release 5 coordinate.
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Polytene chromosome squashes confirmed the presence of the deletion and showed the cytological breakpoints of Df(3R)BSC138 to be 95A2-7;95A5-B1. (95A1,2 and 95B1,2 were present. Either 95A4,5 or 95A7,8 was absent, but it was not possible to tell from the chromosome spreads which doublet was still present.)