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.
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
An incorrect lefthand progenitor insertion of P{XP}Dokd02937, and thus an incorrect sequence location for breakpoint 1 of X:7 ,113,595 and an incorrect estimated cytology for the left end of segment 1 of 7A4, were displayed on FlyBase through to the FB2010_02 release.
Carries two copies of a mini-w marker.
The cytological breakpoints of Df(1)BSC711 predicted from the Release 5 genomic coordinates of the progenitor insertion sites are 7B1;7C1.