[38F5-38F5];[39D2-39D2];
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.
38F5;39D2
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG31673EP432 and P{PZ}l(2)38EFd04530 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k14505k14505&P{lacW}l(2)k05106k05106 and P{PZ}l(2)05095a05095a