[39A1-39A1];[39A6-39A6];
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.
39A1;39A6
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Lethal in combination with Df(2L)G5.1.
Fails to complement Df(2L)Exel7080.
Inferred to overlap with: Df(2L)Exel7080.
Presence of P+PBac{XP5.WH5}BSC302 was verified using the PCR methods and primers described in FBrf0175003.
Cytological breakpoints of Df(2L)BSC302 predicted from the progenitor P{XP}CG9265d00690 and PBac{WH}CG9249f00835 genome coordinates are 39A1;39A6.