[19F1-19F1];[19F6-19F6];
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.
19F1;19F6
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}CG1702EP1525 and P{EP}EP1465&P{EP}CG1486EP1192