Table 3

Array-based comparative genomic hybridisation result overview in PLB

(A) Most recurrent chromosomal alterations in PLB (losses and gains are separated)
Chromosome bandStart cloneEnd cloneStart position (bp)End position (bp)Size (bp)CNANo of cases
1p36.3–1p35.1RP4-785P20RP1-117N332145213337965030165129Loss5
6q14.1–6q27RP11-25O6RP5-1086L228340549417050977987104285Loss4
14q32.33RP11-417P24CTC-820M161052673581062781731010815Loss7
15q11.2–15q26.5RP11-289D12RP11-14C102036371710003618479672467Loss5
1q21.1–1q44.1RP3-365I19RP11-438H8142642781247249719104606938Gain5
2p16.1–2p15RP11-440P5RP11-479F13605018006142244920349Amplification4
6p21.31RP11-175A4RP1-90K1033521322370777733556451Gain4
7p22–7q36.2RP11-449P15RP11-518I12885103157752947156867844Gain6
(B) Candidate genes residing in frequently altered regions
ChromosomeChromosome bandSize (bp)CNANo of casesCancer gene census
11p36.3–1p35.130165129Loss5LCK, MDS2, SDHB, PRDM16, PAX7
1414q32.331010815Loss7IGH
22p16.1–2p15920349Amplification4REL, BCL11A
66p21.313556451Gain4HMGA1, SFRS3, FANCE
  • CNA, copy number alteration.