[87C7-87C7];[87D7-87D7];
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.
87C7;87D7
Inferred to overlap with: Df(3R)Exel7318.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Confirmed by PCR (using the 3-step process described on http://www.drosdel.org.uk/del_confirm.php).
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}Vha55j2E9 and P{PZ}CtBP03463