[97D2-97D2];[97F1-97F1];
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.
97D2;97F1
Inferred to overlap with: Df(3R)BSC791.
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{lacW}scribj7B3 and P{lacW}His2AvL1602 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}sda03884 and P{PZ}btzrL203