Table 2.
NP | P neg | P dys | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Chr | Location | Cytoband | Gain/Loss | freq | foot pvalue | freq | foot pvalue | freq | foot pvalue | Genes of Interest | ||
1 | NP only | 4 | 28Mb | 4p15.1 | gain | 25.0% | 0.002 | |||||
7 | 9Mb | 7p21 | loss | 25.0% | 0.034 | NXPH1 | ||||||
9 | 91Mb | 9q22 | loss | 25.0% | 0.010 | SPIN1, SHC3 | ||||||
2 | P neg only | 11 | 64Mb | 11q13 | gain | 20% | 0.002 | COX8A, BAD, NRXN2, MAP4K2 | ||||
15 | 19Mb | 15q11.2 | gain | 20% | 0.010 | |||||||
2 | 25Mb | 2p23 | loss | 20% | 0.010 | CENPO, ADCY3 | ||||||
3 | P dys | 6 | 20Mb | 6p22 | gain | 20% | 0.008 | E2F3 | ||||
10 | 24Mb | 10p12 | gain | 20% | 0.002 | ARHGAP21 | ||||||
5 | 133Mb | 5q31 | loss | 20% | 0.048 | SKP1, VDAC1, PPP2CA | ||||||
7 | 129Mb | 7q32 | loss | 20% | 0.044 | MIR183 | ||||||
4 | P neg & dys | 2 | 230–231Mb | 2q36 | loss | 30% | 0.020 | 30% | 0.004 | FBXO36 | ||
3 | 171Mb | 3q26 | loss | 30% | 0.010 | 30% | 0.004 | TNIK, PLD1, FNDC3B | ||||
3 | 44Mb | 3p21 | loss | 40% | 0.020 | 30% | 0.020 | KIF15 | ||||
4 | 173Mb | 4q34 | loss | 40% | 0.020 | 50% | 0.006 | GALNTL6 | ||||
4 | 4–5Mb | 4p16.2 | loss | 20% | 0.010 | 40% | 0.004 | STX18 | ||||
15 | 69–70Mb | 15q22 | loss | 50% | 0.020 | 60% | 0.004 | MIR629 | ||||
16 | 6Mb | 16p13 | loss | 30% | 0.010 | 20% | 0.124 | A2BP1 | ||||
5 | NP & P | 1 | 103–104Mb | 1p21 | loss | 37.5% | 0.004 | 40% | 0.010 | 50% | 0.004 | COL11A1 |
2 | 233Mb | 2q37 | loss | 25.0% | 0.002 | 20% | 0.090 | 30% | 0.004 | ALPI | ||
3 | 8Mb | 3p26 | loss | 37.5% | 0.002 | 40% | 0.020 | 30% | 0.032 | RAD18 | ||
6 | 16–18Mb | 6p22 | loss | 37.5% | 0.004 | 40% | 0.010 | 30% | 0.002 | ATXN1 | ||
9 | 9Mb | 9p23 | loss | 25.0% | 0.054 | 30% | 0.050 | 50% | 0.004 | PTPRD |
Frequency of regions of copy gain and copy loss as detected by STAC analysis for UC non-progressors (n=9; left), and UC progressors (n=11) at non-dysplastic (middle columns) or dysplastic (right columns) sites as indicated by cytoband and genomic location (NCBI Build 36.3). Number of samples and relative percentage (in parentheses) are shown for each alteration per group. Data is grouped to reflect sites specific to one or more of the sample sets (non-progressor, NP; progressor, P; progressor (dysplasia), P dys). NS = p-value > 0.05; not significant.