[38D1-38D1];[38F5-38F5];
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.
38D1;38F5
Homozygous Df(2L)ED1317 embryos produce an abnormality in which intersegmental (ISNb) axons form loops on muscles 6 and 7.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}k02501&P{lacW}k14810 and P{PZ}Hr3802306&P{PZ}dia1 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG31673EP432 and P{PZ}l(2)38EFd04530