[30B12-30B12];[30C1-30C1];
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.
30B12;30C1
Homozygous Df(2L)ED684 mutant embryos display intersegmental nerve b (ISNb) defects.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-HA-1721 and P{RS3}CB-0705-3.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{EP}Oatp30BEP890 and P{EP}EP361&P{EP}peloEP2160