[11A1-11A1];[11B14-11B14];
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.
11A1;11B14
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP1451&P{EP}EP1629 and P{EP}CG11138EP1313 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG11138EP1313 and P{EP}EP1632&P{EP}EP1449