Table II.

Summary of CNAs detected by array-comparative genomic hybridization.

Chromosome (alteration U or R)	Cytobands	NCBI36/hg18	Size of imbalance (Mb)	Online Mendelian Inheritance in Man genes
5 (U)	del(5)(q31.3q32)	chr5:142,130,476-145,871,262	3.74	ARHGAP26, NR3C1, HMHB1, YIPF5, KCTD16, PRELID2, GRXCR2, SH3RF2, PLAC8L1, LARS, RBM27, POU4F3, TCERG1
9 (R)	del(9)(p21.3p21.3)	chr9:21,212,342-22,632,472	1.42	IFNA17, IFNA14, IFNA22P, IFNA5, KLHL9, IFNA6, IFNA13, IFNA2, IFNA8, IFNA1, MIR31HG, IFNE, MIR31, MTAP, CDKN2A-DT, CDKN2A, CDKN2B-AS1, CDKN2B, DMRTA1
9 (U)	del(9)(q33.3q33.3)	chr9:124,813,871-125,060,804	0.24	RABGAP1, GPR21, MIR600HG, STRBP
22 (U)	del(22)(q11.22q11.22)	chr22:20,811,200-21,422,368	0.61	VPREB1, BMS1P20, ZNF280B, ZNF280A, PRAME, LL22NC03-63E9.3, POM121L1P, GGTLC2

R and U acquired CNAs are correspondingly highlighted in the first column. Results obtained are presented using standard gene abbreviations and such used according to the international system of cytogenomic nomenclature. CNAs, copy number alterations; R, recurrent; U, unique.