Table 2.

Most frequently gained clones in MCL


Clone name

Base position, Kb

Cytogenetic band

% of cases with copy number gain

Genes in affected interval
Group A     
RP11-79f11*  Chr3: 165,285   3q26.1   83  SI, BCHE 
RP11-21j16   Chr8: 116,016   8q23.3   77  TRPS1 
RP11-90m7   Chr3: 164,334   3q26.1   75   —  
RP11-80f24   Chr8: 78,335   8q21.12   69   —  
RP11-89i16   Chr8: 114,648   8q23.3   69   —  
RP11-90d3   Chr4: 43,447   4p13   64   —  
RP11-89e20   Chr3: 112,456   3q13.13   64  PVRL3, CD96, TACTILE 
RP11-91f9   Chr3: 119,136   3q13.32   62   —  
RP11-91f17   Chr3: 167,543   3q26.1   57  SI, BCHE 
Group B     
RP11-90e13*  Chr4: 171,790   4q33   85   —  
RP11-54818   Chr12: 55,220   12q13.2   75  NEUROD4, HEM1, DCD 
RP11-75h6   Chr19: 0,988   19p13.3   73  DRIL 1, CNN2, STK11 
RP11-91i19   Chr4: 144,372   4q31.21   69  INPP4B, HP43, SNARCA5 
RP11-14k17   Chr11: 39,871   11p12   69   —  
RP11-111p16   Chr6: 55,523   6p12.1   69  BMP5, COL21A1 
RP11-91o1   Chr13: 89,942   13q31.3   69  GPC5 
RP11-89a6   Chr15: 54,253   15q21.3   69  TCF12, AQP9 
RP11-88n10   Chr12: 88,021   12q21.32   67  KITLG 
CTD-2101j13   Chr12: 88,824   12q21.3   64  DUSP6, TUWD12, KITLG 
RP11-142f22   Chr8: 100,581   8q22.2   64  COX6, RNF19, SPAG1 
RP11-171g12   Chr4: 181,787   4q34.3   62   —  
RP11-35p16   Chr16: 4,580   16p13.3   62  GLIS2, HMOX2, DNAJA3 
RP11-71f18   Chr7: 19,239   7p21.1   62  HDAC9, TWIST1, FERD3L 
RP11-131k16   Chr4: 121,820   4q27   57  MAD2L1, PRDM5 
Group C     
RP11-91a22   Chr16: 46,347   16q11.2   86  SHCBP1, VPS35, GPT2 
RP11-91m10   Chr11: 85,444   11q14.1   77  DLG2 
RP11-229a12   Chr3: 57,333   3p14.3   75  DNAH12, SLMAP, ARF 4 
RP11-172k14
 
Chr5: 74,567
 
5q13.3
 
62
 
HEXB, EFG2, POLK, F2R
 

Clone name

Base position, Kb

Cytogenetic band

% of cases with copy number gain

Genes in affected interval
Group A     
RP11-79f11*  Chr3: 165,285   3q26.1   83  SI, BCHE 
RP11-21j16   Chr8: 116,016   8q23.3   77  TRPS1 
RP11-90m7   Chr3: 164,334   3q26.1   75   —  
RP11-80f24   Chr8: 78,335   8q21.12   69   —  
RP11-89i16   Chr8: 114,648   8q23.3   69   —  
RP11-90d3   Chr4: 43,447   4p13   64   —  
RP11-89e20   Chr3: 112,456   3q13.13   64  PVRL3, CD96, TACTILE 
RP11-91f9   Chr3: 119,136   3q13.32   62   —  
RP11-91f17   Chr3: 167,543   3q26.1   57  SI, BCHE 
Group B     
RP11-90e13*  Chr4: 171,790   4q33   85   —  
RP11-54818   Chr12: 55,220   12q13.2   75  NEUROD4, HEM1, DCD 
RP11-75h6   Chr19: 0,988   19p13.3   73  DRIL 1, CNN2, STK11 
RP11-91i19   Chr4: 144,372   4q31.21   69  INPP4B, HP43, SNARCA5 
RP11-14k17   Chr11: 39,871   11p12   69   —  
RP11-111p16   Chr6: 55,523   6p12.1   69  BMP5, COL21A1 
RP11-91o1   Chr13: 89,942   13q31.3   69  GPC5 
RP11-89a6   Chr15: 54,253   15q21.3   69  TCF12, AQP9 
RP11-88n10   Chr12: 88,021   12q21.32   67  KITLG 
CTD-2101j13   Chr12: 88,824   12q21.3   64  DUSP6, TUWD12, KITLG 
RP11-142f22   Chr8: 100,581   8q22.2   64  COX6, RNF19, SPAG1 
RP11-171g12   Chr4: 181,787   4q34.3   62   —  
RP11-35p16   Chr16: 4,580   16p13.3   62  GLIS2, HMOX2, DNAJA3 
RP11-71f18   Chr7: 19,239   7p21.1   62  HDAC9, TWIST1, FERD3L 
RP11-131k16   Chr4: 121,820   4q27   57  MAD2L1, PRDM5 
Group C     
RP11-91a22   Chr16: 46,347   16q11.2   86  SHCBP1, VPS35, GPT2 
RP11-91m10   Chr11: 85,444   11q14.1   77  DLG2 
RP11-229a12   Chr3: 57,333   3p14.3   75  DNAH12, SLMAP, ARF 4 
RP11-172k14
 
Chr5: 74,567
 
5q13.3
 
62
 
HEXB, EFG2, POLK, F2R
 

In group A, hotspots are present in the smallest regions of overlap. In group B, hotspots are present in consecutive areas. In group C, hotspots are not present in any of the consecutive areas. Mb positions of the clones were determined with USSC genome browser (April 2003 freeze). Hotspots were defined as clones with a ratio >0.3 in 8 or more of the 14 cases. Percentages were calculated by dividing the number of cases with ratio >0.3 with the number of samples that gave a hybridization signal. RP11-79f11 and RP11-91f17, RP11-89i16 and RP11-21j16, RP11-88n10 and CTD-2101j13 are consecutive clones. Genes were identified in the Mb region between the flanking clones of a hotspot.

— indicates that there are no known genes in the interval.

*

These clones were identified as polymorphisms in the human genome by either Sebat et al27  or lafrate et al.28 

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