[51C5-51C5];[51F11-51F11];
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.
51C5;51F11
Df(2R)hbs-j5/Df(2R)ED2423 mutants display a reduction in bristle numbers on the thorax compared with wild-type.
Inferred to overlap with: Df(2R)hbs-j5.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-SZ-3694 and P{RS3}CB-0236-3.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}Rpn6k00103 and P{PZ}chn02064 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}scb01288 and P{lacW}dupk03308