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.
Inferred to overlap with: Df(3R)ED5785.
The breakpoints of Df(3R)BSC790 predicted from the Release 5 genomic coordinates of the progenitor PBac{WH}sllf05755 and P{XP}htld07110 transposable element insertion sites are 3R:13432489 ;13875093..13875130 and the cytological breakpoints predicted from these coordinates are 90B6;90E2.