[11B15-11B15];[11E8-11E8];
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.
11B15;11E8
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}UM-8127-3 and P{RS5}5-HA-1738.
Confirmed by 3-step PCR confirmation as shown in 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}CG11138EP1313 and P{EP}EP1632&P{EP}EP1449 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP1461 and P{EP}CG1640EP1626