[78D5-78D5];[79A2-79A2];
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.
78D5;79A2
Separable from: kugED4978.
The kugED4978 lesion was identified as a second hit on the Df(3L)ED4978 chromosome.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-SZ-3290 and P{RS3}CB-5230-3.
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