<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>95(10)</volume><submitter>Orsetti B</submitter><pubmed_abstract>Chromosome 1 is involved in quantitative anomalies in 50-60% of breast tumours. However, the structure of these anomalies and the identity of the affected genes remain to be determined. To characterise these anomalies and define their consequences on gene expression, we undertook a study combining array-CGH analysis and expression profiling using specialised arrays. Array-CGH data showed that 1p was predominantly involved in losses and 1q almost exclusively in gains. Noticeably, high magnitude amplification was infrequent. In an attempt to fine map regions of copy number changes, we defined 19 shortest regions of overlap (SROs) for gains (one at 1p and 18 at 1q) and of 20 SROs for losses (all at 1p). These SROs, whose sizes ranged from 170 kb to 3.2 Mb, represented the smallest genomic int</pubmed_abstract><journal>British journal of cancer</journal><pagination>1439-47</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2360604</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genetic profiling of chromosome 1 in breast cancer: mapping of regions of gains and losses and identification of candidate genes on 1q.</pubmed_title><pmcid>PMC2360604</pmcid><pubmed_authors>Rouge C</pubmed_authors><pubmed_authors>Theillet C</pubmed_authors><pubmed_authors>Nguyen C</pubmed_authors><pubmed_authors>Orsetti B</pubmed_authors><pubmed_authors>Chuchana P</pubmed_authors><pubmed_authors>Bibeau F</pubmed_authors><pubmed_authors>Rodriguez C</pubmed_authors><pubmed_authors>Cervera N</pubmed_authors><pubmed_authors>Lasorsa L</pubmed_authors><pubmed_authors>Ursule L</pubmed_authors><pubmed_authors>Nugoli M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic profiling of chromosome 1 in breast cancer: mapping of regions of gains and losses and identification of candidate genes on 1q.</name><description>Chromosome 1 is involved in quantitative anomalies in 50-60% of breast tumours. However, the structure of these anomalies and the identity of the affected genes remain to be determined. To characterise these anomalies and define their consequences on gene expression, we undertook a study combining array-CGH analysis and expression profiling using specialised arrays. Array-CGH data showed that 1p was predominantly involved in losses and 1q almost exclusively in gains. Noticeably, high magnitude amplification was infrequent. In an attempt to fine map regions of copy number changes, we defined 19 shortest regions of overlap (SROs) for gains (one at 1p and 18 at 1q) and of 20 SROs for losses (all at 1p). These SROs, whose sizes ranged from 170 kb to 3.2 Mb, represented the smallest genomic int</description><dates><release>2006-01-01T00:00:00Z</release><publication>2006 Nov</publication><modification>2026-04-08T02:41:42.352Z</modification><creation>2019-03-27T02:44:55Z</creation></dates><accession>S-EPMC2360604</accession><cross_references><pubmed>17060936</pubmed><doi>10.1038/sj.bjc.6603433</doi></cross_references></HashMap>