[21B3-21B3];[21B7-21B7];
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.
21B3;21B7
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-0416-3 and P{RS5}5-SZ-3580.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}spenk06805&P{lacW}l(2)k13604k13604 and P{lacW}U2af38k14504