[7E11-7E11];[8A2-8A2];
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.
7E11;8A2
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Df(1)BSC592/Df(1)BSC627 embryos display axon guidance defects.
Inferred to overlap with: Df(1)BSC627.
The presence of P+PBac{XP5.WH5}BSC592 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(1)BSC592 predicted from the Release 5 genomic coordinates of the progenitor insertions are 7E11;8A2.