[96A7-96A7];[96C3-96C3];
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.
96A7;96C3
Inferred to overlap with: Df(3R)BSC679.
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 of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}crb07207&P{PZ}BRWD305842 and P{EP}CycB3EP3127 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}OstStt3j2D9 and P{PZ}Aats-gln05461