. 2006 Sep;174(1):271–284. doi: 10.1534/genetics.106.058099

TABLE 2.

High-resolution QTL mapping from complementation tests of deficiencies

Chromosome	Deficiency name	P-value L × G	QTL	No. of loci^b
X	Df(1)JC70/FM7c	0.0004	4F11–5A2	43
2	Df(2L)S2590/CyO	0.0039	23D2–23E3	53
2	Df(2L)ed-dp/SM1	0.0024	24C3–24E4	73
2	Df(2L) Trf-C6R31/CyO	0.0078	28C1–28E7	106
2	Df(2L)XE-2750/CyO	0.0004	28C1–28E7	106
2	Df(2L)Prl/CyO	0.0001	32F1–33B3	58
2	Df(2L)TE35BC-24/CyO	0.0001^a	35B10–35D1	37
2	Df(2L)H20/CyO	0.0064^a	36D1–36E2	29
2	Df(2L)prA16/CyO	0.0001^a	37B2–37F1	175
2	DF(2l)TW158/CyO	0.0022	37B2–37F1	175
2	Df(2L)TW161/CyO	0.0001^a	38B1–40B1	407
2	Df(2R)ST1/CyO	0.0008	42B3–42E1	87
3	Df(3R)Dr-rv1/TM3	0.0001	99A6–99C1	87
3	Df(3R)01215/TM3	0.0083	99A6–99C1	87
3	Df(3R)faf-BP/TM6B	0.0048	100D2–100F5	66
3		Df(3R)04661/TM3	100D2–100F5	66	0.0003^a

Significant L × G × S interaction in addition to significant L × G term.

Number of genes in QTL intervals based on Drysdale et al. (2005).