Dan at 18:48, 22 January 2026

2026-01-22T18:48:03Z

← Older revision		Revision as of 13:48, 22 January 2026
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	~~'''Welcome to the CCGA!'''~~		=TEST SITE=

	*An open resource focused on describing clinically relevant chromosomal and genomic abnormalities in cancer		*An open resource focused on describing clinically relevant chromosomal and genomic abnormalities in cancer

Dan: Created page with "'''Welcome to the CCGA!''' An open resource focused on describing clinically relevant chromosomal and genomic abnormalities in cancer Intended as a companion resource to the [https://tumourclassification.iarc.who.int/welcome/ WHO Classification of Tumours (WCT)] book series Provides clinically significant genetic information for entities based on the current WCT disease ontology Supported by the [https://www.cancergenomics.org/ Cancer Genomics Consortium (C..."

2026-01-22T18:47:45Z

Created page with "'''Welcome to the CCGA!''' *An open resource focused on describing clinically relevant chromosomal and genomic abnormalities in cancer *Intended as a companion resource to the [https://tumourclassification.iarc.who.int/welcome/ WHO Classification of Tumours (WCT)] book series *Provides clinically significant genetic information for entities based on the current WCT disease ontology *Supported by the [https://www.cancergenomics.org/ Cancer Genomics Consortium (C..."

New page

'''Welcome to the CCGA!'''

*An open resource focused on describing clinically relevant chromosomal and genomic abnormalities in cancer
*Intended as a companion resource to the [https://tumourclassification.iarc.who.int/welcome/ WHO Classification of Tumours (WCT)] book series
*Provides clinically significant genetic information for entities based on the current WCT disease ontology
*Supported by the [https://www.cancergenomics.org/ Cancer Genomics Consortium (CGC)] and in collaboration with [https://whobluebooks.iarc.fr/about/ IARC] (publisher of the WCT book series)
*Crowdsourced using a wiki-style interface, allowing for real-time editing and content sharing
*Contributed to by colleagues with an interest in clinical cytogenetics, molecular genetics and genomics in cancer ([https://mms.cancergenomics.org/members/form.php?orgcode=CGC&fid=3830649 Volunteer Form])

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[[File:CGC logo only.png|100px|link=Main_Page]]<span id="fp-span-cgc-pre"> '''CGC Workgroups Recurrent Loci Tables'''</span><span id="fp-span-cgc" style="display: inline-block; margin-left: 30px;"> [[AML Table: Recurrent Genomic Alterations Detected by Chromosomal Microarray|AML]] | [[MDS, MDS/MPN and MPN Tables: Recurrent Genomic Alterations Detected by Chromosomal Microarray|MDS/MPN]] | [[CLL Tables: Regions of Recurrent Copy Number Change and CN-LOH|CLL]] | [[Recurrent Genomic Alterations in Pediatric and Adult Central Nervous System Tumors Detected by Chromosomal Microarray|CNS Tumors]] | [[Plasma Cell Neoplasms Tables: Recurrent Cytogenomic Alterations|Plasma Cell Neoplasms]] | [[Breast Cancer: Recurrent Genomic Alterations|Breast Cancer]] | [[Renal Cell Neoplasia Tables: Recurrent Cytogenomic Alterations|Renal Neoplasia]] | [[B-ALL Tables: Prognostic Genomic Abnormalities and Recurrent Gene Fusions|B-ALL]]</span>
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<h4>Author Resources</h4>
- [[Author Instructions]]

- [[Video Tutorials]]

- [[Volunteer_Assignments_and_Opportunities|Authorship Assignment]]
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<h4>Join Us!</h4>
- [[About Us]]

- [https://mms.cancergenomics.org/members/form.php?orgcode=CGC&fid=3830649 Volunteer Form]

- [[Description_of_CCGA_Roles|Role Descriptions]]
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<h4>Frequently Asked Questions</h4>
- [[Frequently Asked Questions (FAQs)|FAQs]]

- [[Contact us|Contact Us]]
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The Compendium Of Cancer Genome Aberrations - Revision history

Dan at 18:48, 22 January 2026