[78A2-78A2];[78C2-78C2];
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.
78A2;78C2
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(3L)BSC449.
The presence of P+PBac{XP5.WH5}BSC553 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(3L)BSC553 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}CG12984f06763 and P{XP}d09074 transposable element insertion sites are 78A2;78C2.