[21F1-21F1];[22A1-22A1];
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.
21F1;22A1
Lethal in combination with Df(2L)Exel7006.
Df(2L)ED108 homozygous embryos exhibit mild axon guidance defects in the medial tracts, as compared to controls.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k09610k09610&P{lacW}Sk09538a and P{PZ}l(2)1068510685&P{lacW}Tango14k00619 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(2)1068510685&P{lacW}Tango14k00619 and P{lacW}RFeSPk11704