Changes

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!Notes
 
!Notes
 
|-
 
|-
|<span class="blue-text">EXAMPLE:</span>
+
|Not found
7
+
|N/A
|<span class="blue-text">EXAMPLE:</span> Loss
+
|N/A
|<span class="blue-text">EXAMPLE:</span>
+
|N/A
chr7:1-159,335,973 [hg38]
+
|N/A
|<span class="blue-text">EXAMPLE:</span>
+
|N/A
chr7
+
|N/A
|<span class="blue-text">EXAMPLE:</span> Yes
+
|
|<span class="blue-text">EXAMPLE:</span> Yes
  −
|<span class="blue-text">EXAMPLE:</span> No
  −
|<span class="blue-text">EXAMPLE:</span>
  −
Presence of monosomy 7 (or 7q deletion) is sufficient for a diagnosis of AML with MDS-related changes when there is ≥20% blasts and no prior therapy (add reference).  Monosomy 7/7q deletion is associated with a poor prognosis in AML (add reference).
  −
|-
  −
|<span class="blue-text">EXAMPLE:</span>
  −
8
  −
|<span class="blue-text">EXAMPLE:</span> Gain
  −
|<span class="blue-text">EXAMPLE:</span>
  −
chr8:1-145,138,636 [hg38]
  −
|<span class="blue-text">EXAMPLE:</span>
  −
chr8
  −
|<span class="blue-text">EXAMPLE:</span> No
  −
|<span class="blue-text">EXAMPLE:</span> No
  −
|<span class="blue-text">EXAMPLE:</span> No
  −
|<span class="blue-text">EXAMPLE:</span>
  −
Common recurrent secondary finding for t(8;21) (add reference).
   
|}
 
|}
 
==Characteristic Chromosomal Patterns==
 
==Characteristic Chromosomal Patterns==
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|}Note: A more extensive list of mutations can be found in cBioportal (https://www.cbioportal.org/), COSMIC (https://cancer.sanger.ac.uk/cosmic), ICGC (https://dcc.icgc.org/) and/or other databases. When applicable, gene-specific pages within the CCGA site directly link to pertinent external content.
 
|}Note: A more extensive list of mutations can be found in cBioportal (https://www.cbioportal.org/), COSMIC (https://cancer.sanger.ac.uk/cosmic), ICGC (https://dcc.icgc.org/) and/or other databases. When applicable, gene-specific pages within the CCGA site directly link to pertinent external content.
 
==Epigenomic Alterations==
 
==Epigenomic Alterations==
Put your text here
+
N/
 
==Genes and Main Pathways Involved==
 
==Genes and Main Pathways Involved==
 
Put your text here and fill in the table <span style="color:#0070C0">(''Instructions: Can include references in the table. Do not delete table.'')</span>
 
Put your text here and fill in the table <span style="color:#0070C0">(''Instructions: Can include references in the table. Do not delete table.'')</span>
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Put your text here
 
Put your text here
 
==Familial Forms==
 
==Familial Forms==
Put your text here <span style="color:#0070C0">(''Instructions: Include associated hereditary conditions/syndromes that cause this entity or are caused by this entity.'') </span>
+
<span style="color:#0070C0">N/A </span>
 
==Additional Information==
 
==Additional Information==
Put your text here
+
N/A
 
==Links==
 
==Links==
 
(use the "Link" icon that looks like two overlapping circles at the top of the page) <span style="color:#0070C0">(''Instructions: Highlight text to which you want to add a link in this section or elsewhere, select the "Link" icon at the top of the page, and search the name of the internal page to which you want to link this text, or enter an external internet address by including the "<nowiki>http://www</nowiki>." portion.'')</span>
 
(use the "Link" icon that looks like two overlapping circles at the top of the page) <span style="color:#0070C0">(''Instructions: Highlight text to which you want to add a link in this section or elsewhere, select the "Link" icon at the top of the page, and search the name of the internal page to which you want to link this text, or enter an external internet address by including the "<nowiki>http://www</nowiki>." portion.'')</span>
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