Table 7 Array comparative genome hybridisation results in 16 patients with complex chromosomal rearrangements.

Patient (total no of breakpoints before and after array CGH)	Deleted regions	Non‐deleted probe (Mb)	Deletion start (Mb)	Deletion end (Mb)	Non‐deleted probe (Mb)	Deletion size (Mb)
42 (5,7)	del(13)(q14.11)	37.82	38.049	41.54	41.69	3.5
43 (3,4)	del(4)(q31.21)	144.7	144.8	147.18	147.28	2.38
44 (8,9)	del(X)(p21.1)	32.37	32.42	33.47	33.81	1
45 (4,6)	del(18)(q12.3)	37.4	37.5	38.4	38.5	0.9
46 (4, 6)	del(5)(q22.2)	110.5	110.6	112.95	113.58	2.35
47 (10,14)	del(4)(q32.3)	167.63	168.02	169.57	169.65	1.55
	del(11)(p11.2)	46.19	46.26	46.83	46.91	0.57
48 (6,7)	del(4)(pter‐p15.1)			35.13	35.31	35
49 (6,9)	del(4)(q34.1)	172.97	173.18	175.63	175.78	2.45
	del(4)(q34.3)	178.93	179.23	179.83	180.11	0.6
50 (5,7)	del(6)(q21)	108	108.31	111.53	111.77	3.22
	del(11)(q14.3q21)	88.32	88.64	94	94.17	5.36
51 (4,6)	del(1)(p21.1)	103.05	103.2	106.3	106.5	3.1
	del(2)(q32.1)	181.94	182.1	184.9	184.38	2.8
52 (3,6)	del(1)(p31.3)	63.45	63.54	69.37	69.76	5.83
	del(4)(q24)	103.72	103.84	105.5	105.7	1.66
	del(7)(p21.3)	8.41	8.56	10.75	10.85	2.19
53 (7,14)	del(3)(pter‐p26.1)			4.32	4.38	4.3
	del(4)(q21.3–q22.1)	87.44	87.91	90.15	90.31	2.2
	del(8)(q21.11)	76.08	76.47	78.52	78.80	2.1
	del(9)(q31.1q31.2)	103.78	103.94	106.24	106.42	2.6
55 (4,6)	del(6)(q13–q14.1)	74.42	74.46	77.91	78.22	3.5
57 (10,15)	del(3)(p12.3–p12.1)	76.63	77.29	84.73	85.04	7.44
58 (4,8)	del(5)(q33.3q35.1)	156.06	156.28	169.08	169.60	13.0
	del(6)(q16.1)	97.35	97.45	98.73	99.25	1.2
	del(6)(q25.2)	152.55	152.84	155.22	155.28	2.37
	del(8)(q23.3)	114.52	115.35	118.33	118.61	2.98
59 (5,7)	del(2)((q22.1–q22.2)	141.07	141.82	143.82	144.03	2

CGH, comparative genome hybridisation.

Breakpoints and size of the deletions in 12 patients with phenotypic abnormalities, in 1 normal woman with repeated spontaneous abortions and in 3 prenatal cases without echographic anomalies.

Map positions refer to the Genome Assembly May 2004 (build 35).