[79C2-79C2];[80A4-80A4];
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.
79C2;80A4
Approximately 9% of Df(3L)ED230 mutant embryos have a duplication of the RP2 neuron in one hemisegment and have one missing in the contralateral segment.
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)j1B10j1B10 and P{lacW}l(3)j2C4j2C4