[30C5-30C5];[30F1-30F1];
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.
30C5;30F1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS3}CB-0733-3 and P{RS5}5-SZ-3975.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP361&P{EP}peloEP2160 and P{lacW}zf30Ck02506&P{EP}undEP424 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG5899EP701 and P{EP}CG4747EP594&P{lacW}l(2)k13305k13305