[13C3-13C3];[13F1-13F1];
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.
13C3;13F1
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}hiwEP1308 and P{EP}Ahcy13EP1007 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}BEST:RE35685EP1581&P{EP}sdEP1088 and P{EP}Gβ13FEP1071