[85C3-85C3];[85C3-85C3];
A set of 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. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
85C3;85C3
Inferred to overlap with: Df(3R)BSC666.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(3)L4740L4740 and P{EP}D1EP473