Copy Number

 

The putative cancer-associated PDGs driven by SCNAs in each cancer type were identified by four criteria: 1) located in a peak region of a significantly recurrent focal SNCA locus estimated by the genomic identification of significant targets in cancer (GISTIC2) algorithm, (q≤0.25); 2) altered with high frequency and large amplitude (G-score ≥0.1); 3) mRNA reliably detected in at least 10% of tumor specimens in the given cancer type (90th percentile of FPKM value ≥1); and 4) mRNA significantly and positively correlated with copy numbers (Pearson P-value less than 0.001).

 

Pan-cancer level overall G-score of PDGs that recurrently gained or lost copy number in at least one cancer types


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Overall_Gscore No. of Cancer Types
 HGNC Symbol  Ensembl Gene ID  Amplification  Deletion  Amplification  Deletion 
HMGCS2ENSG00000134240  0.00    0.00    0    0  
WNT2BENSG00000134245  0.00    0.14    0    1  
ADAM30ENSG00000134249  0.00    0.00    0    0  
NGFENSG00000134259  0.00    0.00    0    0  
FKBP11ENSG00000134285  0.00    0.00    0    0  
LDHAENSG00000134333  0.00    0.00    0    0  
SAA2ENSG00000134339  0.00    0.00    0    0  
FSTENSG00000134363  0.00    0.00    0    0  
CFHR4ENSG00000134365  0.00    0.00    0    0  
CFHR5ENSG00000134389  0.00    0.00    0    0  
ERN2ENSG00000134398  0.00    0.00    0    0  
GRPENSG00000134443  0.00    0.00    0    0  
IL15RAENSG00000134470  0.19    0.00    1    0  
CCNHENSG00000134480  0.00    0.29    0    2  
KLRD1ENSG00000134539  0.00    0.00    0    0  
KLRC1ENSG00000134545  0.00    0.00    0    0  
SPXENSG00000134548  0.00    0.00    0    0  
ACP2ENSG00000134575  0.00    0.15    0    1  
STK26ENSG00000134602  0.00    0.00    0    0  
FOLH1BENSG00000134612  0.00    0.00    0    0  

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