[8F9-8F9];[9B1-9B1];
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.
8F9;9B1
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php
Limits computationally determined from location of progenitor P insertion on genome sequence between P{EP}nejEP1149&P{EP}nejEP1179 and P{EP}α-Man-IEP1628&P{EP}α-Man-IEP1307