[76F1-76F1];[77A1-77A1];
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.
76F1;77A1
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(3L)BSC830.
Inferred to overlap with: Df(3L)XS533.
The presence of P+PBac{XP5.WH5}BSC446 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(3L)BSC446 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}f00301 and P{XP}d09071 insertion sites are 76F1;77A1.