[56D10-56D10];[56E2-56E2];
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.
56D10;56E2
Inferred to overlap with: Df(2R)BSC782.
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 of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k00705k00705&P{lacW}mei-W68k05603 and P{EP}CG11007EP736 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}sm05338&P{PZ}emm1 and P{lacW}l(2)k08002k08002