[99A5-99A5];[99C1-99C1];
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.
99A5;99C1;[99A5-99A5];[99C1-99C1];
99A5;99C1
Inferred to overlap with: Df(3R)ED6310.
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}l(3)0470804708 and P{PZ}l(3)0674306743 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)0674306743 and P{PZ}ncd05884