Supplementary Table 6A from High <i>ALK</i> Receptor Tyrosine Kinase Expression Supersedes <i>ALK</i> Mutation as a Determining Factor of an Unfavorable Phenotype in Primary Neuroblastoma
Chromosome 1p LOH was seen in one-third of cases. LOH events on chromosomes 11q and 1p were generally accompanied by copy number loss. The one exception was on chromosome 11p, where LOH in all 4 cases
Patients older than 18 months of age with stage 3, MYCN-non-amplified, unfavorable histology neuroblastoma represent a rare subset of children with outcomes that are inferior to those of most patients
Genome and transcriptome sequence data from a neuroblastoma patient, generated as part of the BC Cancer Agency's Pediatric Personalized Onco-Genomics studyEGA dataset EGAD00001015277
Additional file 9: Supplementary Table 3. COSMIC output. 450 distinct COSMIC mutations found by SCReadCounts to be expressed in at least 4 individual cells in one or more of the 7 neuroblastoma sample
Nucleotide numbering for cDNA –based nomenclature uses 1+ as to the A of the ATG translation initiation codon in Genebank RefSeq NM_004977.2.The initiation codon is codon 1. RefSeq NG_008134.1, NP_004
