[10D6-10D6];[11A1-11A1];
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.
10D6;11A1
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS3}CB-6377-3 and P{RS5}5-HA-1730.
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 of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}bifEP395&P{EP}PhKγEP779 and P{EP}EP345&P{EP}EP1409 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP1451&P{EP}EP1629 and P{EP}CG11138EP1313