[69B5-69B5];[69C4-69C4];
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.
69B5;69C4
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{PZ}l(3)0508805088 and P{PZ}l(3)0692406924