[98F12-98F12];[99B2-99B2];
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.
98F12;99B2
Inferred to overlap with: Df(3R)ED6316.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-SZ-3012 and P{RS3}CB-0479-3.
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{EP}EP3390EP3390 and P{PZ}l(3)0470804708 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