[88A4-88A4];[88C9-88C9];
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.
88A4;88C9
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-8036-3 and P{RS5}5-HA-1073.
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{PZ}flfl01949 and P{lacW}trxj14A6&P{PZ}trx00347 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}put10460 and P{EP}CG33967EP666